Literature DB >> 26442672

Kv3.3 potassium channels and spinocerebellar ataxia.

Yalan Zhang1, Leonard K Kaczmarek1,2.   

Abstract

The voltage-dependent potassium channel subunit Kv3.3 is expressed at high levels in cerebellar Purkinje cells, in auditory brainstem nuclei and in many other neurons capable of firing at high rates. In the cerebellum, it helps to shape the very characteristic complex spike of Purkinje cells. Kv3.3 differs from other closely related channels in that human mutations in the gene encoding Kv3.3 (KCNC3) result in a unique neurodegenerative disease termed spinocerebellar ataxia type 13 (SCA13). This primarily affects the cerebellum, but also results in extracerebellar symptoms. Different mutations produce either early onset SCA13, associated with delayed motor and impaired cognitive skill acquisition, or late onset SCA13, which typically produces cerebellar degeneration in middle age. This review covers the localization and physiological function of Kv3.3 in the central nervous system and how the normal function of the channel is altered by the disease-causing mutations. It also describes experimental approaches that are being used to understand how Kv3.3 mutations are linked to neuronal survival, and to develop strategies for treatment.
© 2015 The Authors. The Journal of Physiology © 2015 The Physiological Society.

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Year:  2015        PMID: 26442672      PMCID: PMC4983625          DOI: 10.1113/JP271343

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  40 in total

Review 1.  Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing.

Authors:  B Rudy; C J McBain
Journal:  Trends Neurosci       Date:  2001-09       Impact factor: 13.837

Review 2.  Non-conducting functions of voltage-gated ion channels.

Authors:  Leonard K Kaczmarek
Journal:  Nat Rev Neurosci       Date:  2006-10       Impact factor: 34.870

Review 3.  More than a pore: ion channel signaling complexes.

Authors:  Amy Lee; Bernd Fakler; Leonard K Kaczmarek; Lori L Isom
Journal:  J Neurosci       Date:  2014-11-12       Impact factor: 6.167

4.  A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.

Authors:  Mikko Muona; Samuel F Berkovic; Leanne M Dibbens; Karen L Oliver; Snezana Maljevic; Marta A Bayly; Tarja Joensuu; Laura Canafoglia; Silvana Franceschetti; Roberto Michelucci; Salla Markkinen; Sarah E Heron; Michael S Hildebrand; Eva Andermann; Frederick Andermann; Antonio Gambardella; Paolo Tinuper; Laura Licchetta; Ingrid E Scheffer; Chiara Criscuolo; Alessandro Filla; Edoardo Ferlazzo; Jamil Ahmad; Adeel Ahmad; Betul Baykan; Edith Said; Meral Topcu; Patrizia Riguzzi; Mary D King; Cigdem Ozkara; Danielle M Andrade; Bernt A Engelsen; Arielle Crespel; Matthias Lindenau; Ebba Lohmann; Veronica Saletti; João Massano; Michael Privitera; Alberto J Espay; Birgit Kauffmann; Michael Duchowny; Rikke S Møller; Rachel Straussberg; Zaid Afawi; Bruria Ben-Zeev; Kaitlin E Samocha; Mark J Daly; Steven Petrou; Holger Lerche; Aarno Palotie; Anna-Elina Lehesjoki
Journal:  Nat Genet       Date:  2014-11-17       Impact factor: 38.330

5.  Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.

Authors:  Michael F Waters; Natali A Minassian; Giovanni Stevanin; Karla P Figueroa; John P A Bannister; Dagmar Nolte; Allan F Mock; Virgilio Gerald H Evidente; Dominic B Fee; Ulrich Müller; Alexandra Dürr; Alexis Brice; Diane M Papazian; Stefan M Pulst
Journal:  Nat Genet       Date:  2006-02-26       Impact factor: 38.330

6.  Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels.

Authors:  Allan F Mock; Jessica L Richardson; Jui-Yi Hsieh; Gina Rinetti; Diane M Papazian
Journal:  BMC Neurosci       Date:  2010-08-16       Impact factor: 3.288

7.  Allele-dependent changes of olivocerebellar circuit properties in the absence of the voltage-gated potassium channels Kv3.1 and Kv3.3.

Authors:  Anne McMahon; Stephen C Fowler; Teresa M Perney; Walther Akemann; Thomas Knöpfel; Rolf H Joho
Journal:  Eur J Neurosci       Date:  2004-06       Impact factor: 3.386

8.  Kv3.3 channels at the Purkinje cell soma are necessary for generation of the classical complex spike waveform.

Authors:  Edward Zagha; Eric J Lang; Bernardo Rudy
Journal:  J Neurosci       Date:  2008-02-06       Impact factor: 6.167

9.  Regulation of Kv channel expression and neuronal excitability in rat medial nucleus of the trapezoid body maintained in organotypic culture.

Authors:  Huaxia Tong; Joern R Steinert; Susan W Robinson; Tatyana Chernova; David J Read; Douglas L Oliver; Ian D Forsythe
Journal:  J Physiol       Date:  2010-03-08       Impact factor: 5.182

10.  Kv3.3b expression defines the shape of the complex spike in the Purkinje cell.

Authors:  Ken Veys; Dirk Snyders; Erik De Schutter
Journal:  Front Cell Neurosci       Date:  2013-11-13       Impact factor: 5.505

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  20 in total

Review 1.  Ion channel dysfunction in cerebellar ataxia.

Authors:  David D Bushart; Vikram G Shakkottai
Journal:  Neurosci Lett       Date:  2018-02-05       Impact factor: 3.046

2.  Editorial.

Authors:  Ian D Forsythe
Journal:  J Physiol       Date:  2016-08-15       Impact factor: 5.182

Review 3.  Kv3 Channels: Enablers of Rapid Firing, Neurotransmitter Release, and Neuronal Endurance.

Authors:  Leonard K Kaczmarek; Yalan Zhang
Journal:  Physiol Rev       Date:  2017-10-01       Impact factor: 37.312

4.  Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia.

Authors:  Ravi Chopra; Aaron H Wasserman; Stefan M Pulst; Chris I De Zeeuw; Vikram G Shakkottai
Journal:  Hum Mol Genet       Date:  2018-04-15       Impact factor: 6.150

5.  Modeling Neurodegenerative Spinocerebellar Ataxia Type 13 in Zebrafish Using a Purkinje Neuron Specific Tunable Coexpression System.

Authors:  Kazuhiko Namikawa; Alessandro Dorigo; Marta Zagrebelsky; Giulio Russo; Toni Kirmann; Wieland Fahr; Stefan Dübel; Martin Korte; Reinhard W Köster
Journal:  J Neurosci       Date:  2019-03-12       Impact factor: 6.167

6.  Suppression of Kv3.3 channels by antisense oligonucleotides reverses biochemical effects and motor impairment in spinocerebellar ataxia type 13 mice.

Authors:  Yalan Zhang; Imran H Quraishi; Heather McClure; Luis A Williams; YungChih Cheng; Siddharth Kale; Graham T Dempsey; Sudhir Agrawal; David J Gerber; Owen B McManus; Leonard K Kaczmarek
Journal:  FASEB J       Date:  2021-12       Impact factor: 5.191

Review 7.  The need for new approaches in CNS drug discovery: Why drugs have failed, and what can be done to improve outcomes.

Authors:  Valentin K Gribkoff; Leonard K Kaczmarek
Journal:  Neuropharmacology       Date:  2016-03-12       Impact factor: 5.250

8.  Kv3.3 Channels Bind Hax-1 and Arp2/3 to Assemble a Stable Local Actin Network that Regulates Channel Gating.

Authors:  Yalan Zhang; Xiao-Feng Zhang; Matthew R Fleming; Anahita Amiri; Lynda El-Hassar; Alexei A Surguchev; Callen Hyland; David P Jenkins; Rooma Desai; Maile R Brown; Valeswara-Rao Gazula; Michael F Waters; Charles H Large; Tamas L Horvath; Dhasakumar Navaratnam; Flora M Vaccarino; Paul Forscher; Leonard K Kaczmarek
Journal:  Cell       Date:  2016-03-17       Impact factor: 41.582

9.  Transduction Profile of the Marmoset Central Nervous System Using Adeno-Associated Virus Serotype 9 Vectors.

Authors:  Yasunori Matsuzaki; Ayumu Konno; Ryo Mukai; Fumiaki Honda; Masafumi Hirato; Yuhei Yoshimoto; Hirokazu Hirai
Journal:  Mol Neurobiol       Date:  2016-02-16       Impact factor: 5.590

10.  Presynaptic Kv3 channels are required for fast and slow endocytosis of synaptic vesicles.

Authors:  Xin-Sheng Wu; Shobana Subramanian; Yalan Zhang; Bo Shi; Jessica Xia; Tiansheng Li; Xiaoli Guo; Lynda El-Hassar; Klara Szigeti-Buck; Jorge Henao-Mejia; Richard A Flavell; Tamas L Horvath; Elizabeth A Jonas; Leonard K Kaczmarek; Ling-Gang Wu
Journal:  Neuron       Date:  2021-01-27       Impact factor: 18.688

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